Colon Cancer: Gene >> HIST1H1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331442
Start	27866887:27866887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.643G>A
AA Mutation	p.Ala215Thr(p.A215T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331442
Start	27867081:27867081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.449A>G
AA Mutation	p.Lys150Arg(p.K150R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331442
Start	27866877:27866877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775091070
CDS Mutation	c.653C>T
AA Mutation	p.Ala218Val(p.A218V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331442
Start	27867151:27867151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.379G>A
AA Mutation	p.Gly127Ser(p.G127S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331442
Start	27867050:27867050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764722398
CDS Mutation	c.480G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331442
Start	27866894:27866894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.636A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331442
Start	27867149:27867149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.381C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331442
Start	27867179:27867179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.351G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331442
Start	27867177:27867178(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.352dupG
AA Mutation	p.Glu118GlyfsTer13(p.E118Gfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HIST1H1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331442
Start	27867042:27867042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.488C>A
AA Mutation	p.Ala163Glu(p.A163E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331442
Start	27867375:27867375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780574435
CDS Mutation	c.155C>T
AA Mutation	p.Ala52Val(p.A52V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331442
Start	27866918:27866918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.612A>T
AA Mutation	p.Lys204Asn(p.K204N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331442
Start	27867348:27867348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.182C>A
AA Mutation	p.Ser61Tyr(p.S61Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331442
Start	27867239:27867239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.291G>A
Mutation Classification	Silent
Feature Type	Transcript